Literature DB >> 34779924

Combination of resveratrol and BIBR1532 inhibits proliferation of colon cancer cells by repressing expression of LncRNAs.

Bakiye Goker Bagca1, Hasan Onur Caglar2, Selin Cesmeli3, Neslihan Pinar Ozates3, Cumhur Gunduz3, Cigir Biray Avci4.   

Abstract

Colorectal cancer (CRC) is the third most common cancer worldwide. The development of tumor drug resistance is observed in the treatment of CRC. Combinations of anticancer agents are attracting considerable interest in order to overcome drug resistance in CRC. This study aims to investigate the effect of resveratrol and BIBR1532, either alone or in combination, on the cell viability as well as on expression of long non-coding RNAs (LncRNAs) for HT-29 colon adenocarcinoma cells. The cytotoxic effects of resveratrol and BIBR1532 on HT-29 cells were determined using WST-1 test. Flow cytometry was used to determine apoptotic cell death after treatments. Real-Time PCR was used to identify expression of LncRNAs after treatments. LncExpDB and GEPIA2 were used to evaluate expression profiles of LncRNAs, whose expression levels were decreased in HT-29 cells after treatments, in normal tissues and colon adenocarcinoma tumors. IC50 concentrations of BIBR1532 and resveratrol were found to be 50.81 μM at 48 h and 86.23 μM at 72 h, respectively. Combination index value was 1.07617. BIBR1532, resveratrol, or their combination reduced the cell viability of HT-29 cells. CCAT1, CRNDE, HOTAIR, PCAT1, PVT1, SNHG16 were down-regulated after treatments. In silico analysis revealed that LncRNAs whose expression levels were decreased after treatments were associated with CRC. Resveratrol, BIBR1532, or their combination may have anti-proliferative effect on colorectal cancer cells through repressing expression of LncRNAs that are involved in progression of CRC.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  BIBR1532; Colorectal cancer; HT29 cells; Long non-coding RNA; Resveratrol

Mesh:

Substances:

Year:  2021        PMID: 34779924     DOI: 10.1007/s12032-021-01611-w

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  55 in total

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Review 3.  Colorectal cancer.

Authors:  Evelien Dekker; Pieter J Tanis; Jasper L A Vleugels; Pashtoon M Kasi; Michael B Wallace
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Journal:  Apoptosis       Date:  2014-07       Impact factor: 4.677

5.  Defective mismatch repair as a predictive marker for lack of efficacy of fluorouracil-based adjuvant therapy in colon cancer.

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7.  Intra-patient Inter-metastatic Genetic Heterogeneity in Colorectal Cancer as a Key Determinant of Survival after Curative Liver Resection.

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Authors:  Reza Bayat Mokhtari; Tina S Homayouni; Narges Baluch; Evgeniya Morgatskaya; Sushil Kumar; Bikul Das; Herman Yeger
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Review 10.  Resveratrol is a promising agent for colorectal cancer prevention and treatment: focus on molecular mechanisms.

Authors:  Mohadese Honari; Rana Shafabakhsh; Russel J Reiter; Hamed Mirzaei; Zatollah Asemi
Journal:  Cancer Cell Int       Date:  2019-07-15       Impact factor: 5.722

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  3 in total

Review 1.  Disease-Associated Regulation of Non-Coding RNAs by Resveratrol: Molecular Insights and Therapeutic Applications.

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Review 2.  Using ncRNAs as Tools in Cancer Diagnosis and Treatment-The Way towards Personalized Medicine to Improve Patients' Health.

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Journal:  Int J Mol Sci       Date:  2022-08-19       Impact factor: 6.208

3.  Resveratrol Improves the Digestive Ability and the Intestinal Health of Siberian Sturgeon.

Authors:  Shiyong Yang; Wenqiang Xu; Langkun Feng; Chaoyang Zhang; Chaozhan Yan; Jiajin Zhang; Jiansheng Lai; Taiming Yan; Zhi He; Xiaogang Du; Zongjun Du; Wei Luo; Xiaoli Huang; Jiayun Wu; Yunkun Li
Journal:  Int J Mol Sci       Date:  2022-10-09       Impact factor: 6.208

  3 in total

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